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AAV Antikörper

Der Maus Monoklonal Anti-AAV-Antikörper wurde für IF, IP, WB, IHC (fro) und EIA validiert. Er ist geeignet, AAV in Proben von Adeno-Associated Virus (AAV) zu detektieren.
Produktnummer ABIN112133

Kurzübersicht für AAV Antikörper (ABIN112133)

Target

AAV (Adeno-Associated Virus (AAV))

Reaktivität

  • 2
  • 1
  • 1
Adeno-Associated Virus (AAV)

Wirt

  • 2
  • 1
Maus

Klonalität

  • 2
  • 1
Monoklonal

Konjugat

  • 3
Dieser AAV Antikörper ist unkonjugiert

Applikation

Immunofluorescence (IF), Immunoprecipitation (IP), Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Enzyme Immunoassay (EIA)

Klon

A1
  • Aufreinigung

    Protein A Affinity Chromatography

    Immunogen

    Adeno-associated virus capsid proteins and virus Particles.

    Isotyp

    IgG2a
  • Applikationshinweise

    Immunofluorescence microscopy. Immunohistochemistry: 1: 10 - 1: 20, 3 h at room temperature or overnight at 2-8C. Immunoprecipitation. Immunoblotting. ELISA.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Rekonstitution

    Restore with 1 mL dist. water

    Vorsichtsmaßnahmen

    Use of sodium azide as a preservative will substantially inhibit the enzyme activity of horseradish peroxidase.

    Handhabung

    Avoid repeated freezing and thawing.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    AAV (Adeno-Associated Virus (AAV))

    Andere Bezeichnung

    Adeno-Associated Virus

    Substanzklasse

    Virus

    Hintergrund

    Adeno-associated virus (AAV) is a small virus which infects humans and some other primate species. AAV is not currently known to cause disease and consequently the virus causes a very mild immune response. AAV can infect both dividing and non-dividing cells and may incorporate its genome into that of the host cell. These features make AAV a very attractive candidate for creating viral vectors for gene therapy, and for the creation of isogenic human disease models. The capsid proteins: VP1, VP2 and VP3 interact together to form a capsid of an icosahedral symmetry.Synonyms: AAV-2

    UniProt

    O56652
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